Canonical Allele Identifier: PA236997
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 191587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Pro739Ala
CA236993
NM_020297.3:c.2215C>G